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碳负载磁铁矿纳米复合材料在非均相类芬顿反应中对催化活性的结构效应

Structural effects on the catalytic activity of carbon-supported magnetite nanocomposites in heterogeneous Fenton-like reactions.

作者信息

Zang Hongmei, Miao Chunyan, Shang Jianying, Liu Yingxin, Liu Juan

机构信息

The Key Laboratory of Water and Sediment Sciences, Ministry of Education, College of Environmental Sciences and Engineering, Peking University Beijing 100871 China

School of Gemmology, China University of Geosciences Beijing, 100083 China.

出版信息

RSC Adv. 2018 May 1;8(29):16193-16201. doi: 10.1039/c8ra02286k. eCollection 2018 Apr 27.

Abstract

The catalytic reactivity of synthetic bare magnetite nanoparticles, activated carbon supported magnetite (AC-Mt), and graphene oxide supported magnetite (GO-Mt) for heterogeneous Fenton-like oxidation of methylene blue (MB) were compared, in order to investigate how the structural features of the support impact catalytic activity of the nanocomposites. The different effects of AC and GO on MB removal rate, hydroxyl radical (˙OH) production, iron leaching, and surface deactivation have been systematically studied. The rate constant of MB removal by AC-Mt was 0.1161 min, one order of magnitude larger than the value of bare magnetite nanoparticles (0.0566 min). The higher catalytic activity of AC-Mt might be attributed to the larger reactive surface area of well-dispersed magnetite for ˙OH production and the recharge of the magnetite surface by the AC support Fe-O-C bonds. However, the removal rate of MB by GO-Mt was one order of magnitude slower than that of bare magnetite nanoparticles under the same experimental conditions, presumably due to the wrapping of GO around magnetite nanoparticles or extensive aggregation of GO-Mt composites. These findings revealed the significant influence of support structure on the catalytic activity of carbon-supported magnetite nanocomposites, which is important for the development of efficient magnetite-based catalysts for wastewater treatments.

摘要

比较了合成的裸磁铁矿纳米颗粒、活性炭负载磁铁矿(AC-Mt)和氧化石墨烯负载磁铁矿(GO-Mt)对亚甲基蓝(MB)的非均相类芬顿氧化的催化反应活性,以研究载体的结构特征如何影响纳米复合材料的催化活性。系统研究了AC和GO对MB去除率、羟基自由基(˙OH)生成、铁浸出和表面失活的不同影响。AC-Mt去除MB的速率常数为0.1161 min,比裸磁铁矿纳米颗粒的值(0.0566 min)大一个数量级。AC-Mt较高的催化活性可能归因于分散良好的磁铁矿产生˙OH的反应表面积较大,以及AC载体的Fe-O-C键对磁铁矿表面的再充电。然而,在相同实验条件下,GO-Mt对MB的去除率比裸磁铁矿纳米颗粒慢一个数量级,这可能是由于GO包裹在磁铁矿纳米颗粒周围或GO-Mt复合材料的广泛聚集。这些发现揭示了载体结构对碳负载磁铁矿纳米复合材料催化活性的显著影响,这对开发用于废水处理的高效磁铁矿基催化剂很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eac4/9080278/3a59da62dc0a/c8ra02286k-f1.jpg

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